Product Recalls in South Dakota

Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,273 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,273 in last 12 months

Showing 13011320 of 47,632 recalls

Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 Recalled by Olympus Corporation of the...

The Issue: Additional IFU updates to provide further clarification on safe and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Boston Scientific Corporation

Recalled Item: CXR Preconnect with TENACIO Pump with InhibiZone Recalled by Boston...

The Issue: The potential for devices to experience inflation and/or deflation...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2025· Boston Scientific Corporation

Recalled Item: CX Preconnect with TENACIO Pump without InhibiZone Recalled by Boston...

The Issue: The potential for devices to experience inflation and/or deflation...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS BF-XT190 Recalled by Olympus...

The Issue: Additional IFU updates to provide further clarification on safe and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Insulet Corporation

Recalled Item: The failure occurs if a user on the Omnipod 5 Recalled by Insulet...

The Issue: The failure occurs if a user on the Omnipod 5 iOS application selects and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2025· Medline Industries, LP

Recalled Item: Medline Adult Anesthesia Set Recalled by Medline Industries, LP Due to...

The Issue: Specific items and lots of Medline Kits may contain Clearlink IV Sets which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2025· MedicalCommunications GmbH

Recalled Item: Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version Recalled by...

The Issue: Potential that the measured value may be smaller than the actual area.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2025· Biomet, Inc.

Recalled Item: Juggerknot Mini Soft Anchors Recalled by Biomet, Inc. Due to The outer...

The Issue: The outer carton box label is for the JuggerKnot 1.0mm Mini products....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock Closed Vial Spike Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock Vented Vial Spike Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical 45" (114 cm) Appx 1.7 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock Bag Spike Recalled by ICU Medical, Inc. Due to Port...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Oncology Kit w/ChemoLock Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Double ChemoLock Port Syringe Transfer Set Recalled by ICU...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemosafeLock Bag Spike Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· Beckman Coulter, Inc.

Recalled Item: CellMek SPS Sample Preparation System Recalled by Beckman Coulter, Inc. Due...

The Issue: Automated pipetting, diluting and specimen processing workstations for flow...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemosafeLock Vial Adapter : KL-VA001U3 KL-VA002U3 KL-VA131U3...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Oncology Kit w/2 ChemoLock" Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock Vented Vial Spike Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Chemo Lock Universal Vented Vial Spike Recalled by ICU Medical,...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing